| Large-scale whole-genome sequencing of the Icelandic population DF Gudbjartsson, H Helgason, SA Gudjonsson, F Zink, A Oddson, ... Nature genetics 47 (5), 435-444, 2015 | 874 | 2015 |
| The nature of nurture: Effects of parental genotypes A Kong, G Thorleifsson, ML Frigge, BJ Vilhjalmsson, AI Young, ... Science 359 (6374), 424-428, 2018 | 861 | 2018 |
| Large-scale integration of the plasma proteome with genetics and disease E Ferkingstad, P Sulem, BA Atlason, G Sveinbjornsson, MI Magnusson, ... Nature genetics 53 (12), 1712-1721, 2021 | 595 | 2021 |
| Characterizing mutagenic effects of recombination through a sequence-level genetic map BV Halldorsson, G Palsson, OA Stefansson, H Jonsson, MT Hardarson, ... Science 363 (6425), eaau1043, 2019 | 285 | 2019 |
| Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits U Styrkarsdottir, G Thorleifsson, P Sulem, DF Gudbjartsson, A Sigurdsson, ... Nature 497 (7450), 517-520, 2013 | 283 | 2013 |
| The sequences of 150,119 genomes in the UK Biobank BV Halldorsson, HP Eggertsson, KHS Moore, H Hauswedell, O Eiriksson, ... Nature 607 (7920), 732-740, 2022 | 280 | 2022 |
| Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease A Helgadottir, S Gretarsdottir, G Thorleifsson, E Hjartarson, A Sigurdsson, ... Nature genetics 48 (6), 634-639, 2016 | 259 | 2016 |
| Identification of a large set of rare complete human knockouts P Sulem, H Helgason, A Oddson, H Stefansson, SA Gudjonsson, F Zink, ... Nature genetics 47 (5), 448-452, 2015 | 258 | 2015 |
| Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits D Beyter, H Ingimundardottir, A Oddsson, HP Eggertsson, E Bjornsson, ... Nature genetics 53 (6), 779-786, 2021 | 240 | 2021 |
| Weighting sequence variants based on their annotation increases power of whole-genome association studies G Sveinbjornsson, A Albrechtsen, F Zink, SA Gudjonsson, A Oddson, ... Nature genetics 48 (3), 314-317, 2016 | 214 | 2016 |
| Loss-of-function variants in ATM confer risk of gastric cancer H Helgason, T Rafnar, HS Olafsdottir, JG Jonasson, A Sigurdsson, ... Nature genetics 47 (8), 906-910, 2015 | 180 | 2015 |
| Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis U Styrkarsdottir, SH Lund, G Thorleifsson, F Zink, OA Stefansson, ... Nature genetics 50 (12), 1681-1687, 2018 | 175 | 2018 |
| Common and rare variants associated with kidney stones and biochemical traits A Oddsson, P Sulem, H Helgason, VO Edvardsson, G Thorleifsson, ... Nature communications 6 (1), 7975, 2015 | 153 | 2015 |
| A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis RP Kristjansson, S Benonisdottir, OB Davidsson, A Oddsson, V Tragante, ... Nature genetics 51 (2), 267-276, 2019 | 113 | 2019 |
| The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms A Oddsson, SY Kristinsson, H Helgason, DF Gudbjartsson, G Masson, ... Leukemia 28 (6), 1371-1374, 2014 | 108 | 2014 |
| A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis S Bell, AS Rigas, MK Magnusson, E Ferkingstad, E Allara, G Bjornsdottir, ... Communications biology 4 (1), 156, 2021 | 105 | 2021 |
| A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease GA Arnadottir, GL Norddahl, S Gudmundsdottir, AB Agustsdottir, ... Nature Communications 9 (1), 4447, 2018 | 105 | 2018 |
| Identification of sequence variants influencing immunoglobulin levels S Jonsson, G Sveinbjornsson, AL de Lapuente Portilla, B Swaminathan, ... Nature genetics 49 (8), 1182-1191, 2017 | 103 | 2017 |
| A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation DF Gudbjartsson, H Holm, P Sulem, G Masson, A Oddsson, ... European heart journal, ehw379, 2016 | 101 | 2016 |
| Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits T Rafnar, B Gunnarsson, OA Stefansson, P Sulem, A Ingason, ML Frigge, ... Nature communications 9 (1), 3636, 2018 | 100 | 2018 |
Daniel GudbjartssonStatistician, Decode GeneticsVerified email at decode.is
